Crossword Puzzle: Newborn Screening (Ma. Mikee Raven R Castillo, 2-BSMT)

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Across
  1. 1. The lead agency responsible for newborn screening in the Philippines (3 letters)
  2. 3. Deficiency in this enzyme results in Carnitine Palmitoyl-Transferase Type 1 Deficiency (9 letters)
  3. 5. The primary organ affected in Tyrosinemia Type I (5 letters)
  4. 6. A condition characterized by elevated methionine (12 letters)
  5. 9. Deficiency in this enzyme causes Isovaleric Acidemia (10 letters)
  6. 14. Acronym for National Institutes of Health (3 letters)
  7. 17. Blood is collected on a ________ card for testing (7 letters)
  8. 19. Group of disorders including Citrullinemia and Argininosuccinic Aciduria (4 letters)
  9. 20. This transport defect is also known as Carnitine Transporter Deficiency (3 letters)
  10. 21. This acid builds up in Phenylketonuria (12 letters)
  11. 22. Neonatal onset and cardiomyopathy are signs of this fatty acid disorder (4 letters)
  12. 23. Physical deformity or death may result from untreated heritable ________ (10 letters)
  13. 24. Essential hormone affected in Congenital Hypothyroidism (8 letters)
  14. 25. Severe ________ may lead to coma and death in organic acidurias (7 letters)
  15. 27. Essential amino acid affected in Thalassemias (6 letters)
  16. 29. Neonates with Carnitine Uptake Defect may not have the condition but reflect low levels from their ________ (6 letters)
  17. 32. A process of testing newborns for heritable conditions (9 letters)
  18. 33. One of the disorders detected by newborn screening involves low ________ sugar (5 letters)
  19. 35. In Hemoglobinopathies, structural abnormalities arise due to single ________ substitutions (5 letters)
  20. 36. The condition where the body fails to breakdown fat for energy (9 letters)
  21. 37. A vitamin important in Multiple Carboxylase Deficiency (6 letters)
  22. 39. Neonates with MSUD often have elevated ________ levels (7 letters)
Down
  1. 2. The advisory committee includes members like pediatricians and ________ (12 letters)
  2. 4. Document acknowledging refusal of newborn screening is kept in the newborn’s ________ record (8 letters)
  3. 7. The condition also known as Richner-Hanhart Syndrome (11 letters)
  4. 8. A complication of untreated Congenital Adrenal Hyperplasia in girls (11 letters)
  5. 10. Genomic term describing diseases like Hemoglobinopathies (7 letters)
  6. 11. Symptoms of Galactosemia include elevated ________ levels (9 letters)
  7. 12. Common metabolic crisis symptom in Methylmalonic Acidemia (8 letters)
  8. 13. The state shall ________ and promote the right to health (7 letters)
  9. 15. Term for enlarged adrenal glands in CAH (10 letters)
  10. 16. Enzyme deficient in Maple Syrup Urine Disease (6 letters)
  11. 18. Refusal of testing must be based on ________ beliefs (9 letters)
  12. 26. Deficiency in this enzyme causes Glutaric Aciduria Type I (15 letters)
  13. 28. Failure to thrive is a symptom in ________ Acidemia (13 letters)
  14. 29. Disease causing a "sweet-smelling" urine (4 letters)
  15. 30. Biochemical testing for ________ conditions (9 letters)
  16. 31. Infants with Biotinidase Deficiency cannot recycle this coenzyme (6 letters)
  17. 34. Urea Cycle Defect results in an increase of ________ in the blood (7 letters)
  18. 38. Abbreviation for Very Long Chain Acyl-CoA Dehydrogenase Deficiency (4 letters)